Canonical Allele Identifier: CA486173237

Gene: SOS2

Linked Data

• COSMIC: COSM469996 ; COSM469997
• MyVariant Identifiers: chr14:g.50597307T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130589T>A , CM000676.2:g.50130589T>A	GRCh38
NC_000014.8:g.50597307T>A , CM000676.1:g.50597307T>A	GRCh37
NC_000014.7:g.49667057T>A	NCBI36
NG_051073.1:g.106105A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3249A>T MANE Select	ENSP00000216373.5:p.Pro1083=
ENST00000216373.9:c.3249A>T	ENSP00000216373.5:p.Pro1083=
ENST00000543680.5:c.3150A>T	ENSP00000445328.1:p.Pro1050=
NM_006939.2:c.3249A>T	NP_008870.2:p.Pro1083=
XM_005268021.1:c.3069A>T	XP_005268078.1:p.Pro1023=
XM_011537103.1:c.3210A>T	XP_011535405.1:p.Pro1070=
NM_006939.3:c.3249A>T	NP_008870.2:p.Pro1083=
NM_006939.4:c.3249A>T MANE Select	NP_008870.2:p.Pro1083=